A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6030934



Internal ID21940277
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:48220200..48232844hg38UCSC Ensembl
chr15:48512397..48525041hg19UCSC Ensembl
Cytoband15q21.1
Allele length
AssemblyAllele length
hg3812645
hg1912645
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17612058
Samples
Known GenesSLC12A1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6030934
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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